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Nadia Bahi-Buisson

Showing results (11-20 of 174) with videos related to

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Developmental Medicine and Child Neurology|February 5, 2009
The ketogenic diet improves recently worsened focal epilepsyNathalie Villeneuve, Florence Pinton, Nadia Bahi-Buisson, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndromeYann Fichou, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 22, 2010
Developmental and benign movement disorders in childhoodCecilia Bonnet, Agathe Roubertie, Diane Doummar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 29, 2018
Polysomnographic findings in Rett syndromeAlessandro Amaddeo, Livio De Sanctis, Jorge Olmo Arroyo, et al.
Pediatric Neurology|February 7, 2006
Misleading effects of clonazepam in symptomatic electrical status epilepticus during sleep syndromeNadia Bahi-Buisson, Rosanna Savini, Monica Eisermann, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Linking MECP2 and pain sensitivity: the example of Rett syndromeJenny Downs, Sandrine M Géranton, Ami Bebbington, et al.
European Journal of Human Genetics : EJHG|April 5, 2012
The phenotype associated with a large deletion on MECP2Ami Bebbington, Jenny Downs, Alan Percy, et al.
Molecular Genetics and Metabolism|June 12, 2019
Clinical, biochemical and genetic characteristics of a cohort of 101 French and Italian patients with HPRT deficiencyAnnalisa Madeo, Maja Di Rocco, Anaïs Brassier, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathyJuliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
Pageof 18

Showing results (11-20 of 174) with videos related to

Sort By:
Pageof 18
Developmental Medicine and Child Neurology|February 5, 2009
The ketogenic diet improves recently worsened focal epilepsyNathalie Villeneuve, Florence Pinton, Nadia Bahi-Buisson, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
Mutation in the SLC9A6 gene is not a frequent cause of sporadic Angelman-like syndromeYann Fichou, Nadia Bahi-Buisson, Juliette Nectoux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 22, 2010
Developmental and benign movement disorders in childhoodCecilia Bonnet, Agathe Roubertie, Diane Doummar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 29, 2018
Polysomnographic findings in Rett syndromeAlessandro Amaddeo, Livio De Sanctis, Jorge Olmo Arroyo, et al.
Pediatric Neurology|February 7, 2006
Misleading effects of clonazepam in symptomatic electrical status epilepticus during sleep syndromeNadia Bahi-Buisson, Rosanna Savini, Monica Eisermann, et al.
Neurogenetics|November 27, 2008
The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoformYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Linking MECP2 and pain sensitivity: the example of Rett syndromeJenny Downs, Sandrine M Géranton, Ami Bebbington, et al.
European Journal of Human Genetics : EJHG|April 5, 2012
The phenotype associated with a large deletion on MECP2Ami Bebbington, Jenny Downs, Alan Percy, et al.
Molecular Genetics and Metabolism|June 12, 2019
Clinical, biochemical and genetic characteristics of a cohort of 101 French and Italian patients with HPRT deficiencyAnnalisa Madeo, Maja Di Rocco, Anaïs Brassier, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 26, 2010
Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathyJuliette Nectoux, Yann Fichou, Nicolas Cagnard, et al.
Pageof 18